Halogenated aryloxyacetyl cyanamides as herbicides

ABSTRACT

A series of halogenated aryloxyacetyl cyanamides has been provided. These compounds are characterized by unique biological properties, and it has been found that members of the series provided herein are outstanding herbicides.

United States Patent Breuer 14 1 M111. 1, 11972 [54] HALOGENATED ARYLOXYACETYL 2,709,648 5/1955 Rykeret a1. ..71/97 CYANAMIDES AS HERBICIDES 2,927,126 3/1960 Pursglove ...71/105 2,949,354 8/1960 l'odd ..71/97 Inventor: Herman Brew, Regensburg, Germany 3,439,018 4/1969 Brookes et a1. ..71/105 [73] Assigneez Olin Chemical Co" Inc. 3,457,294 7/1969 Crovetti et al. ..71/105 3,518,077 6/1970 Berliner et al..... ...71/118 [22] Filed: Aug. 29, 1969 3,557,209 1/1971 Richter et al. ..71/105 1 1 pp N91 872,796 OTHER PUBLICATIONS Related US. Application Data Howard et a1., Amino-N-cyanocarboxyamides, etc.," (l965)(pp.959 961) [60] D1v1s1on of Ser. No. 674,008, Oct. 9, 1967, Pat. No.

3,524,607, Contmuation-m-part of Ser. No. 566,480, Primary Examiner LeWi$ 6on5 July 1966 abandoned Assistant Examiner-G. Hollrah Attorney-Th0mas P. ODay, Gordon D. Byrkit, Donald F. [52] U.S.C| ..7l/97,7l/94, 71/118, Clements, Richard Strickler, George J Koeser d R 71/D1G. l, 260/294.9, 424/263, 424/287, 424/289, lskander 424/292, 424/324 [51] 1lnt.Cl. ..A0ln 9/20 57 ABSTRACT [58] Field oiSearch ...71/105,97,118,120

A serles of halogenated aryloxyacetyl cyanamides has been 56 Rf d provided. These compounds are characterized by unique I 1 e erences l e biological properties, and it has been found that members of UNITED STATES PATENTS the series provided herein are outstanding herbicides.

2,412,510 12/1946 Jones ..7l/ll8 lSClaims,No1Drawings:

HALOGENATED ARYLOXYACETYL CYANAMIDES AS HERBICIDES This application is a division of my copending application Ser. No. 674,008, filed Oct. 9, i967, and now US. Pat. No. 3,524,607 which was a continuation-in-part of my copending application Ser. No. 566,480, filed July 20, 1966, and now abandoned.

This invention relates to the preparation of selected acyl cyanamides having the following general formula:

wherein R represents a halogenated aryl moiety; R represents hydrogen or an alkyl group; and R" represents hydrogen, alkyl, aryl, aralkyl or a selected metal.

Certain acyl cyanamides have been previously prepared and described in the literature. Thus, for instance, the preparation of p-chlorobenzoyl cyanamide has been described by Howard and Youngblood in J. Org. Chem. 31 (1966) page 959. However, the preparation of substituted acyl cyanamides having a halogenated aryloxyacetyl moiety attached to the cyanamide group has not heretofore been accomplished. In accordance with this invention, a series of substituted cyanamides of this nature has now been provided, and the members of the group I are characterized by outstanding herbicidal activity. They are particularly attractive herbicides since they selectively destroy weeds in crop areas without substantially affecting the crops.

The preparation of most of the compounds included in the general formula I proceeds in accordance with the usual procedures involved in preparing acyl cyanamides; that is, they are provided by the reaction of cyanamide or salts thereof with acid chlorides preferably in the presence of a suitable base.

Thus the preferred technique for providing the compounds I wherein R and R are as previously defined and wherein R" is hydrogen involves reacting cyanamide or salts thereof with substituted acyl halides of the formula:

in the presence of a base in order to facilitate the reaction. Although any halide (e.g., fluoride, bromide, iodide, chloride) may be used in the preparation of the products of this invention, the substituted acyl chlorides of the formula II (Wherein X is Cl) are preferred reactants in view of their easy availability and lower price.

The group R in the starting reactant ll represents any halogenated aryl group. As used in the specification and claims herein, the term aryl represents a group not containing any unsaturation other than of the benzenoid type. A preferred embodiment of this invention involves the preparation of the compounds I (using reactants ll) wherein the aryl portion of said R has from 6-10 carbon atoms such as, for instance, phenyl, tolyl, xylyl, naphthyl and the like. In addition these aryl moieties must contain at least one ring substituted halogen substituent such as chlorine, bromine, fluorine and iodine.

Also useful as starting reactants in the preparation of the products of this invention are those reactants ll wherein R represents either hydrogen or lower alkyl 1-4 carbon atoms). Preferred practice involves, however, employing the substituted acyl halides ll wherein R' represents hydrogen.

Illustrative of the reactants encompassed by the general formula ll which may be used in preparation of the products of this invention are, for example: o-chlorophenoxyacetyl chloride, o-fluorophenoxyacetyl chloride, o-bromophenoxyacetyl chloride, o-iodophenoxyacetyl chloride, rn chlorophenoxyacetyl chloride, m-fluorophenoxyacetyl chloride, m-bromophenoxyacetyl chloride, m-iodophenoxyacetyl chloride, p-chlorophenoxyacetyl chloride, pfluorophenoxyacetyl chloride, p-bromophenoxyacetyl chloride, p-iodophenoxyacetyl chloride, 2,4-dichlorophenoxyacetyl chloride, 2,4-dibromophenoxyacetyl chloride, 2,4- diiodophenoxyacetyl chloride, 2,4-difluorophenoxyacetyl chloride, 2-chloro-3-bromophenoxyacetyl chloride, 2-bromo- 4-chlorophenoxyacetyl chloride, 2,S-dichlorophenoxyacetyl chloride, 2,5-difluorophenoxyacetyl chloride, 2-bromo5- chlorophenoxyacetyl chloride, 2,6-dichlorophenoxyacetyl chloride, 2,6-dibromophenoxyacetyl chloride, 2,6- diiodophenoxyacetyl chloride, 2,6-difluorophenoxyacetyl chloride, 3,4-dichlorophenoxyacetyl chloride, 3,4- dibromophenoxyacetyl chloride, 3,4-diiodophenoxyacetyl chloride, 3,S-dichlorophenoxyacetyl chloride, 3,5- dibromophenoxyacetyl chloride, 3,5-diiodophenoxyacetyl chloride and 3bromo-5-chlorophenoxyacetyl chloride.

Similarly, among the useful reactants which may be utilized in the practice of this invention are 2,3,5trichlorophenox yacetyl chloride, 2,4,6-trichlorophenoxyacetyl chloride, 4,6- dichloro-2-bromophenoxyacetyl chloride, 2,6-dichloro-4- bromophenoxyacetyl chloride, 6chloro-2,4-dibromophenoxyacetyl chloride, 2,4,6-tribromophenoxyacetyl chloride, 2,3,S-tribromophenoxyacetyl chloride, 2,3,5-triiodophenoxyacetyl chloride, 2,4,6-triiodophenoxyacetyl chloride, 4-

chloro-2,6dibromophenoxyacetyl chloride, 6-fluoro-2,4- dibromophenoxyacetyl chloride, 4-fluoro-2,6- dibromophenoxyacetyl chloride, 4fluoro-2,6-

dichlorophenoxyacetyl chloride, 2,3,4-,6-tetrachlorophenoxyacetyl chloride, 2,3,4,6-tetrabromophenoxyacetyl chloride,

2,4,6-trichloro-3-bromophenoxyacetyl chloride, 2,3,5- trichloro-4-iodophenoxyacetyl chloride, 3-fluoro-2,4,6- tribromophenoxyacetyl chloride, 3-fluoro-2,4,6-

trichlorophenoxyacetyl chloride, pentachlorophenoxyacetyl chloride, pentabromophenoxyacetyl chloride, 2,4,5,6- tetrachloro-3-bromophenoxyacetyl chloride, 2-methyl-4- chlorophenoxyacetyl chloride, 2-methyl'4-fluorophenoxyacetyl chloride, Z-methyl-4-bromophenoxyacetyl chloride, and Z-methyl-4iodophenoxyacetyl chloride.

Likewise, 4'flu0ro-( l-naphthyloxy)acetyl chloride, 2- chloro-( l-naphthyloxy)acetyl chloride, 8-chloro-( lnaphthyloxy)acetyl chloride, 4-bromo-( l-naphthyloxy)acetyl chloride, l-chloro-(2-naphthyloxy)acetyl chloride, 4-chloro- (2-naphthyloxy)acetyl chloride, l,3-dichloro-(2-naphthyloxy)acetyl chloride, l,4-dichloro-l2-naphthyloxy)acetyl chloride, l,4,6-trichloro-(2-naphthyloxy)acetyl chloride, 1- chloro-6-bromo-(2-naphthyloxy)acetyl chloride, 2-(p chlorophenoxy)propionyl chloride, 2-(2,4-dichlorophenoxy)propionyl chloride, 2-(ochlorophenoxy)butyryl chloride, 2(p'chlorophenoxy)hexanoyl chloride, and 2-(2,4- dichlorophenoxy)-hexanoyl chloride may be utilized as starting reactants.

Preferred embodiments of this invention include those compounds of the general formula I wherein said R group is a chlorinated aryl group containing from 1-5 chlorine atoms substituted on the aryl ring.

The acylation procedure for providing the compounds I wherein R" represents hydrogen is conveniently performed by reacting the aforementioned acid halides ll with cyanamide or salts thereof in an aqueous-organic medium such as water ad mixed with various inert organic solvents including acetone, dioxane and the like. A typical suitable reaction medium is a 30 percent acetone solution in water. A reaction temperature range of about lO C. to about 50 C. is preferentially employed in the acylation process. Stoichiometric quantities of cyanamide and acid chloride may be: employed, although suitably slight molar excesses of cyanamide up to about 20 percent over the stoichiometric amount may be utilized. As mentioned in the preceding discussion, the process is preferably carried out in the presence of a base such as an alkali metal or an alkaline earth metal hydroxide for best results. It has been found that a molar excess of such base is preferably employed, and at least 2 moles of said base/mole of cyanamide reactant should be utilized for optimum yield of product. The base forms a salt both with liberated hydrogen halide and with the provided substituted cyanamide product wherein said product remains in desired solution. Upon completion of the reaction period, the reaction mixture is usually filtered to remove insoluble impurities prior to obtaining the desired product by acidification of the filtrate. The halogenated aryloxyacetyl cyanamide products are then readily isolated by conventional filtration procedures.

The compounds of formula 1 wherein R and R are as previously represented and R is hydrogen are thus provided in accordance with the above procedure. Other procedures are then followed to provide the halogenated aryloxyacetyl cyanamides having the formula 1 wherein R" represents an alkyl group. For instance, the compounds 1 wherein R" represents hydrogen are readily reacted with alkylating agents known to those skilled in this art such as the dialkyl sulfates. Preferred embodiments of this invention are obtained when dialkyl sulfates are employed in this manner wherein the alkyl substituents have l-4 carbon atoms such as dimethyl sulfate.

Alternatively, the compounds encompassed by the formula 1 wherein R represents alkyl, aryl or aralkyl are also provided by first preparing the appropriate alkyl, aryl or aralkyl cyanamides, making the alkali metal salts of said cyanamides and acylating said salts with the aforementioned halogenated aryloxyacetyl chlorides. Preferred embodiments of this invention include those compounds of formula I where R is phenyl or benzyl.

The compounds of the general formula 1 wherein R" represents hydrogen are acidic in nature, and they are readily converted to salts which are also useful agricultural chemicals. Thus, those halogenated aryloxyacetyl cyanamides 1 (wherein R is hydrogen) are easily reacted with the alkali metal hydrides to provide useful herbicides. Any of the alkali metal hydroxides may be used in this manner including lithium, sodium, potassium, cesium and rubidium hydroxides; but preferred embodiments of this invention include the potassium salts. in a similar fashion, the alkaline earth metal (Ca, Sr, Ba) salts also are readily obtainable; and it has been demonstrated that these salts are characterized by outstanding herbicidal properties. Likewise, the compounds 1 wherein R" represents other metals of group 11 in the periodic table such as zinc, magnesium and cadmium are easily provided in accordance with this invention.

Organic bases may also be reacted with the compounds I (wherein R" is hydrogen) to provide salts having good utility as herbicides. For instance, tertiary amines such as trialkyl amines (e.g., triethylamine) may be utilized in such salt preparations as well as other commonly used organic bases such as pyridine and the like. The various ethanolamines may also be employed in the preparation of useful salts in accordance with the invention disclosed herein.

The following examples serve to further illustrate the preparation of the novel products of this invention. However, it is understood that these examples are not to be considered as limiting the scope of this invention in any manner and are furnished merely for the purpose of illustration.

EXAMPLE 1 A solution of 277.2 g. (4.2 moles) of 85 percent potassium hydroxide in 2 liters of water was cooled to 25 C., and 200 g. (2.3 moles) of 50 percent aqueous cyanamide was added. The stirred solution was then maintained at -15 C. while a solution of 410 g. (2.0 moles) of o-chlorophenoxyacetyl chloride in 400 ml. of acetone was added. After addition, the easily stirred slurry was stirred an additional half hour and Analysis.Calcd. for C H ClN O C, 51.30

; H, 3.32; N, 13.30. Found: 0,5121; 11, 3.20; N, 13.24. 7

EXAMPLE 2 One hundred and nine grams (2.6 moles) of anhydrous cyanamide was dissolved in 2,450 ml. of water, and 262 ml. of 30 percent sodium hydroxide solution was added to the cyanamide solution. The resulting solution was cooled to 5-0 C and then with stirring and cooling 532 g. (2.6 moles) of pchlorophenoxyacetyl chloride in 735 ml. of acetone was added dropwise to the first solution. Concurrently, 262 ml. of 30 percent sodium hydroxide was added to the cyanamide solution, and both additions were completed in about 1 hour. The resulting reaction mixture was then stirred for 30 additional minutes. Filtration of the reaction mixture removed a small amount of solid impurities. The clear filtrate was acidified with concentrated hydrochloric acid while maintaining the temperature at 0 C. A precipitate formed, was filtered off, washed with water, and dried in air to provide 516 g. of a fine white powder melting at l24126 C. Elemental analysis confirmed that the desired p-chlorophenoxyacetylcyanamide had been obtained.

EXAMPLE 3 A stirred solution of 138.6 g. (2.1 moles) of percent potassium hydroxide in 1 liter of water was cooled to 25 C. and 46.2 g. (1.1 moles) of anhydrous cyanamide added. The solution was cooled to 10 C. and kept at 1015 C. while 239.5 g. (1.0 mole) of crude 2,4-dichlorophenoxyacetyl chloride in 200 ml. of acetone was added. Within a short time the amount of potassium salt was too thick for good stirring and additional water was added. At the end of addition of the chloride, 3 liters more of water had been added and stirring was still difficult.

The thick mass was acidified with g. 1.2 moles) of concentrated hydrochloric acid. The filtered, water washed solid was air dried. The yield of nearly colorless solid was 226 g. (92.2 percent); m.p. 127130 C. Recrystallization of 50 g. from ethanol, with charcoal treatment, gave 22.0 g.; m.p. 136137 C. The following analytical data revealed that 2,4- dichlorophenoxyacetylcyanamide had been obtained.

Analysis.Calcd. for C H Cl N2O C, 44.08; H, 2.44;

EXAMPLE 4 To a cold solution of 277.2 g. (4.2 moles) of 85 percent potassium hydroxide in 3 liters of water was added 200 g. (2.3 moles) of 50 percent aqueous cyanamide. The stirred solution was maintained at 1520 C. while a solution of 548 g. (2.0 moles) of 2,4,5-trichlorophenoxyacetyl chloride in 300 ml. of acetone was added. After addition, the thick slurry was stirred 15 minutes and acidified with cold, dilute hydrochloric acid. The nearly colorless solid was filtered, washed with water, and air dried. The product weighed 501 g. (89.6 percent); m.p. l70173 C.

For purification, 85 g. of the crude material was heated with ml. of ethanol. lnsolublcs (trimer) were present and removed by filtration. The filtrate was poured into ice water, giving a gum which solidified on standing. The material weighed 44 g. and melted at ll9 l23 C., with appreciable softening below this temperature. A second recrystallization from chloroform with charcoal treatment, gave 14.9 g. of product; m.p. 9798 C. Elemental analysis confirmed that the desired 2,4,5-trichlorophenoxyacetylcyanamide had. been obtained in this latter product.

EXAMPLE 5 A stirred solution of 277.2 g. (4.2 moles) of 85 percent potassium hydroxide in 2 liters of water was cooled to 25 C. and 200 g. (2.3 moles) of 50 percent aqueous cyanamide added. The stirred solution was cooled further and kept at l0-l5 C. while a solution of 438 g. (2.0 moles) of 2-methyl- 4-chlorophenoxyacetyl chloride in 400 ml. of acetone was added. The solution was then stirred one-half hour longer and acidified with cold, dilute hydrochloric acid. The resulting tan precipitate was filtered, washed with water, and air dried. The crude weigh was 439 g. (97.7 percent yield); m.p. 128l32 C. A portion of 60 g. was recrystallized from chloroform with charcoal treatment giving 37.8 g. of off-white crystals; m.p. l42l43 C. The following analytical data revealed that 2- methyl-4-chlorophenoxyacetyl-cyanamide had been obtained.

Analysis-Salad. for C H CIN O I C, 53.45; H 4.00; Cl, 15.81; N, 12.47. Found: C, 53.59; 11, 3.86; Cl, 15.69; N, 12.49.

EXAMPLE 6 A solution of 42.1 g. (0.20 mole) of p-chlorophenoxyacetylcyanamide in 250 ml. of water, containing 13.2 g. (0.20 mole) of 85 percent potassium hydroxide was heated to boiling, charcoaled, and filtered. Dimethylsulfate (26.4 g.; 0.21 mole) was added to the filtrate and the mixture stirred and heated to reflux. Within a short time a heavy oil separated. The mixture was refluxed an hour, poured into ice, and the solid recovered. The crude yield was 23.0 g. (51.2 percent yield; m.p. 8l-89 C.). Purification from ethanol, with charcoal treatment, gave 9.3 g. of off-white crystals; m.p. 91-92 C. The following analytical data revealed that the desired p-chlorophenoxyacetyl-N-methylcyanamide had been obtained.

Analysis.Calcd. for C H ClN O z 53.45; H, 4.00; Cl, 15.81. Found: C, 5288;11, 4.03; Cl, 15.81.

EXAMPLE 7 A solution of 44.9 g. (0.20 mole) of 2-methyl4- chlorophenoxyacetylcyanamide in 250 ml. of water containing 13.2 g. (0.20 mole) of 85 percent potassium hydroxide was heated to boiling, charcoaled, and filtered. After addition of 26.4 g. (0.21 mole) of dimethyl sulfate to the filtrate, the mixture was stirred and refluxed for 30 minutes. The mixture, containing an oil, was poured onto ice. Filtration of the resulting mixture gave 32.7 g. (68.5 percent yield) of tan, sticky solid. Purification from ethanol, with charcoal treatment, gave 9.1 g. of tan crystals melting at 6970 C. Elemental analysis confirmed that 4-chloro-o'tolyloxyacetyll\l-methylcyanamide had been provided in good purity.

EXAMPLE 8 A mixture of 41.9 g. (0.15 mole) of 2,4,5-trichlorophenoxyacetylcyanamide, 9.9 g. (0.15 mole) of 85 percent potassium hydroxide and 200 ml. of water was heated to boiling. The solution was charcoaled and filtered. After addition of 20.1 g. (0.16 mole) of dimethyl sulfate, the mixture was stirred and refluxed for an hour. The resulting heavy oil was poured onto ice and the solid recovered. The crude yield was 37.1 g. (84.3 percent); m.p. 1l0-l 18 C. Recrystallization from ethanol, with charcoal treatment, gave 6.2 g. of product; m.p. l22-12 3 C. The following analytical data revealed that the desired 2,4,S-trichlorophenoxyacetyl-N methylcyanamide had been obtained.

Analysis.-0aled. for (1 11 01 01 0 (J, 40.88; H 2.38; N, 9.54. Found: C, 40.72; 11, 2.56; N, 9.5.).

EXAMPLE 9 A mixture of42.l g. (0.20 mole) of o-chlorophenoxyacetylcyanamide, 13.2 g. (0.20 mole) of 85 percent potassium hydroxide, and 100 ml. of water was heated to boiling, charcoaled, filtered, and cooled. Recovery of off-white salt was 24.0 g. (48.2 percent yield); m.p. 241I242 C. The following analytical data revealed that potassium o-chlorophenoxyacetylcyanamide had been obtained.

A11al vsis.-Calcd. for C H CIN O KI (1, 43.46; H, 2.41; Cl, 14.28. Found: C, 43.80; 11, 2.44; Cl, 14.07.

EXAMPLE 10 A mixture of 42.1 g. (0.20 mole) of p-chlorophenoxyacetylcyanamide, 13.2 g. (0.20 mole) of 85 percent potassium hydroxide, and 100 ml. of water was heated to boiling, charcoaled, and the solution filtered. After cooling, the crystals were filtered, and air dried. Recovery was 21.5 g. (43.2 percent yield) m.p. 260-26l C. The following analytical data revealed that potassium p-chlorophenoxyacetylcyanamide had been obtained.

Analysis.Calecl for ogn olNzozK; c, 43.46; 11

2.41; N, 11.26. Found: C, 43.53; H, 2.57; N, 11.41.

3,04,- o'l, 1: 1.52. Found: 0, 4.5.49,- 11, 3.05; C1, 13.54.

EXAMPLE 11 EXAMPLE 12 To a solution of 9.9 g. (0.15 mole) of percent potassium hydroxide in 75 ml. of water was added 41.9 g. (0.15 mole) of 2,4,5-trichlorophenoxyacetylcyanamide. The mixture was heated to boiling, the solution charcoaled, filtered, and cooled. The resulting colorless salt weighed 26.9 g. (53.4 percent yield) and melted at 26l262 C. Elemental analysis revealed that potassium 2,4,5-trichlorophenoxyacetylcyanamide hydrate had been obtained.

EXAMPLE 13 A mixture of 35.9 g. (0.15 mole) of 2-methyl-4- chlorophenoxyacetylcyanamide, 9.9 g. of 85 percent potassium hydroxide, and 75 ml. of water was heated to boiling, charcoaled, filtered, and cooled. Solid failed to separate and 75 ml. of ethanol was added wherein a solid product separated out. The recovered off'white solid weighed 6.4 g.; m.p. 236-237 C. The following analytical data revealed that potassium 2 methyl-4chlorophenoxyacetylcyanamide had been obtained.

Analvsis Oalod. for C H CIN D K: C, 45.71; 11,

EXAMPLE 14 A solution of 3 l .5 g. (0.15 mole) of o-chlorophenoxyacetylcyanamide in 200 ml. of water containing 9.9 g. (0.15 mole) of 85 percent potassium hydroxide was heated to boiling, charcoaled, and filtered. A solution of 17.5 g. (0.08 mole) of zinc acetate dihydrate in 100 ml. of water was added to the filtrate, giving a tan gum. After solidification, the solid was filtered, washed well with water and air dried. The yield was 5.2

g. or 6.5 percent of a tan solid melting at 2l9-220 C. Elemental analysis indicated that this solid was essentially zinc ochlorophenoxyacetylcyanamide hydrated with 6 moles of water.

EXAMPLE A solution of 42.1 g. (0.20 mole) of p-chlorophenoxyacetylcyanamide and 13.2 g. (0.20 mole) of 85 percent potassium hydroxide in 200 ml. of water was heated, charcoaled, and filtered. A solution of 22.0 g. (0.10 mole) of zinc acetate dihydrate in 100 ml. of water was added to the filtrate. A gummy precipitate formed which soon became solid. The

product was filtered, washed well with water, and air dried..

The yield of off-white tetrahydrate was 45.8 g. (82.3 percent yield); m.p. l00-l01 C. Elemental analysis revealed that zinc p-chlorophenoxyacetylcyanamide tetrahydrate had been obtained.

EXAMPLE 16 A solution of 36.7 g. (0.15 mole) of 2,4-dichlor ophenoxyacetylcyanamide and 9.9 g. (0.15 mole) of 85 percent potassium hydroxide in 200 ml. of water was heated, charcoaled,

and filtered. A solution of 17.5 g. (0.08 mole) of zinc acetate dihydrate in 100 ml. of water was added to the filtrate, giving a gummy precipitate. After the gum became solid, the material was filtered, washed with water, and air dried. .The product weighed 29.1 g. (65.9 percent yield) and melted at l22l23 C. Elemental analysis revealed that zinc 2,4-dichlorophenoxyacetylcyanamide dihydrate had been obtained.

EXAMPLE 1? EXAMPLE 18 A mixture of 42.1 g. (0.20 mole) of p-chlorophenoxyacetylcyanamide, 7.7 g. (0.10 mole) of 96 percent calcium hydroxide, and 100 ml. of water was heated to boiling. Almost complete solution occurred. The solution was charcoaled, filtered, and cooled. The recovered product weighed 5.] g. (11.1 percent yield); m.p. 194-l95 C. Elemental analysis revealed that calcium p-chlorophenoxyacetylcyanamide had been obtained.

As noted in the preceding discussion, the halogenated aryloxyacetyl cyanamides l are useful agricultural chemicals. A number of the compounds I are active as insecticides. However, the substituted cyanamides of this invention are charac terized by outstanding properties as herbicides, and it is in this agricultural area that they are most useful.

0 In general, members of the series 1 are quite active in herand duckweed. The substituted cyanamides of this invention are potent broad spectrum herbicides against a wide variety of I the so-called grassy weeds in addition to exerting this same desirable effect upon various broad-leaved weeds. Supplementing this herbicidal activity is the fact that the substituted cyanamides l are selectively phytotoxic, since they do not seriously affect the growth of many cash crops. ln addition, herbicidal activity for these compounds has been demonstrated when they are utilized in both preemergence and postemergence treatment.

The outstanding herbicidal effectiveness for these compounds is surprising and unexpected, since it has been found, for instance, that the somewhat analogous cyanamides having a halogenated aryl group substituted instead of the halogenated aryloxyacetyl group are nearly devoid of herbicidal activity. Thus, for instance, it has been found that pchlorophenoxyacetyl cyanamide is a particularly outstanding herbicide, while p-chlorobenzoyl cyanamide is practically inactive as a herbicide.

The efficacy of the compounds 1 as herbicides has been clearly demonstrated. For instance, a primary screening evaluation revealed that the halogenated aryloxyacetyl cyanamides at a dosage level of 10 pounds/acre were effective in nearly completely inhibiting the growth of a mixture of weeds including rye grass, crab grass, pigweed and mustard representing common species of unwanted plants of both grassy and broad-leaf type. These superior results were obtained when the cyanamides were employed in both preand postemergence treatment.

More advanced testing has confirmed the excellent herbicidal properties exhibited by the members of the series I, and in addition this further testing has revealed the selective nature of the phytotoxicity possessed by these compounds. For instance, greenhouse flats were planted with seeds of different plants including weed and crop species for evaluation of the phytotoxic effect of the compounds I, and the following procedure was utilized in this evaluation. First the soil in the flats was seeded with crop seeds, and these seeds were covered with a layer of soil. Next weed seeds were planted on designated parts of the soil, and these seeds were covered with another layer of soil. The flats were then sprayed with acetone-water solutions of selected members of the series 1 prior to placing the flats in growing rooms maintained at constant conditions of temperature, humidity and lighting to encourage optimum plant growing.After a period of 2V2 weeks, the flats were examined in order to determine the effects of the halogenated aryloxyacetyl cyanamides on the varied weed and crop species which had been planted.

1n the following table wherein the results of this test are tabulated, the plant and weed species are represented by the following letters:

A-crab grass Cmustard D.lohnson grass l-Clinton oats The relative value of each compound with respect to its herbicidal effect on the various plants is indicated by a number as follows:

Ebarnyard grass F-foxtail Gcorn H cotton 0 no phytotoxicity l-4 slight phytotoxicity 5-7 moderate phytotoxicity 8l0 severe phytotoxicity I A TABLE 1 Lbs. per acre A B C D E F G H I p-Chlorophenoxyacetylg cyanamide- 1 10 u 9 1o 10 n 2 10 Zine p-chlprophenoxyacctyl 8 2 cyanamide tetrahydrate. 1 (J 10 g, m 5 n Table l-Continued Lbs. per acre A B C l.) E F G Zine 2, 4diehloropheuoxyacetyl g cyanamide dihdrate. 9 10 9 H 5 6 2, 4, -T1ichlorophenoxyacetyl- 9, i: Z, N-methyleyanamide. I 5

The data in the above table verifies the high activity of members of the series I as preemergence herbicides against a wide variety of weed species. Furthermore, it reveals the selective phytotoxicity exhibited by several of the members when used at varied dosage levels wherein undesired plant growth is effectively inhibited, but the growth of three valuable cash crops (corn, cotton, oats) is not significantly adversely affected.

The outstanding effectiveness of the halogenated aryloxyacetyl cyanamides as herbicides was further verified by a randomized complete block field test in a known corn producing area. P-chlorophenoxyacetyl cyanamide was utilized as the active herbicidal ingredient in this test. This specialized field test was accomplished in the following manner. A test field was di vided into sixteen plots with suitable buffer zones between each plot. P-chlorophenoxyacetyl cyanamide was applied to four plots at a rate of 10 pounds/acre, to four plots at a rate of 5 pounds/acre, and to four plots at a rate of l pounds/acre, while no active herbicidal ingredient was utilized in the remaining four plots. Plot assignments were given randomly. A known amount of corn was planted in each of the sixteen plots, and seven weed species (rye grass, crab grass, pigweed, mustard, Johnson grass, barnyard grass, and foxtail) were seeded randomly over the sixteen plots. After a 6-week growing period. examination of the test plots was carefully made with respect to (a) corn wet weights of one half the corn in each plot without altering row spacing, (b) weed count in two square feet of each plot selected randomly, and (c) an evaluation of the weed and plant conditions in each plot.

With respect to corn wet weight, there was no significant difference between the wet weight of the corn in the control plots and the wet weight of the corn in the plots treated with the p-chlorophenoxyacetyl cyanamide at l pounds/acre.

Weed control in the treated plots was excellent. An average of)? percent of the weeds were controlled in the plots having an active ingredient concentration of 10 pounds/acre, and likewise at 5 pounds/acre there was a 94 percent weed control. At 1 pound/acre there was still a 70 percent weed control.

With respect to general weed and plant conditions, a particularly outstanding result was obtained in the plots containing 1 pound/acre of the active ingredient. There was a very minor phytotoxic effect in these plots on the corn plants while there was a very high herbicidal activity on the grassy and broad-leaf weeds in these plots. in general, the active ingredient did not exhibit any significant phytotoxicity on the corn until a rate of more than 5 pounds/acre was used.

The above tests clearly demonstrate the effectiveness of the substituted cyanamides l as broad spectrum herbicides which may be utilized in either preor post-emergence treatment against both grassy and broadleaf weeds. All of the compounds I are active as herbicides, but especially potent members, and therefore preferred embodiments of this invention include the compounds l wherein R represents chlorinated phenyl, R represents hydrogen, and R" represents either hydrogen, lower alkyl, an alkali metal or a metal of group ll in the periodic table including the alkaline earth metals. Perhaps' the outstanding member of the series which embodies high herbicidal activity along with minimal phytotoxicity against certain cash crops is p-chlorophenoxyacetyl cyanamide.

The agricultural method of this invention thus comprises applying a herbicidal amount of the substituted cyanamides l to the locus to be protected from undesirable weed growth; for example, it is applied directly to weeds in postemergence treatment and to soil areas in preemergence treatment.

Although the herbicides I may be directly administered to the area where control of weed growth is desired, they are preferably admixed with carriers and diluents which are commonly referred to as pest control adljuvants. Thus a wide variety of such adjuvants may be utilized with the herbicides of this invention to provide herbicidal formulations conveniently adapted for application using conventional applicator equipment. In this respect, both solid and liquid herbicidal formulations containing a member of the series I as the essential active ingredient are provided in accordance with this invention.

For example, dust compositions are readily provided by mixing the active substituted cyanamides l with various frecfiowing solid carriers and grinding the resulting mixture to obtain a dust having an average particle size of about 20-50 microns. Concentration by weight of the active ingredient in these dusts is generally in the range of about 5-20 percent although larger concentrations may be utilized if desired. Among the solid carriers which may be employed in such formulations are natural clays such as attapulgite and kaolinite clays, diatomaceous earth, finely divided talcs and synthetic mineral fillers derived from silica and silicate such as synthetic fine silica and synthetic calcium and magnesium silicates. Other suitable carriers include magnesium and calcium carbonates.

The compounds I may be advantageously formulated with other carriers to provide wettable powders. These powders are conveniently prepared by mixing the active ingredient with solid carriers of the aforementioned type and adding to the mixture a surface-active agent in amount sufficient to impart water dispersibility to the powdered compositions. Aqueous dispersions of such wettable powders are particularly adapted for spraying and sprinkling operations on areas which are to be protected from weed growth.

Numerous surface-active agents are available and suitable for use in such wettable powders. These agents may be referred to as wetting or dispersing agents, and they may be of the nonionic, cationic or anionic type. Mixtures of such agents are conveniently employed in these formulations in a manner well known to those skilled in this art. For example. among those surface-active agents commonly employed in these compositions are alkyl aryl sulfonates such as sodium decyl benzene sulfonate, fatty alcohol sulfates such as sodium dodecyl sulfate, alkali metal oleates, sodium lignosulfonate and the like. A comprehensive listing of many other surfaceactive agents suitable for use in the formulation of typical agricultural dispersions, suspensions, etc., has been prepared and disclosed by McCutcheon in Soap and Chemical Specialties," 3l, Nos. 7-10 i955).

Wettable powders of the above type will usually contain about 0.ll0.0 percent by weight of the aforementioned surface-active agents with the preferred concentration naturally being dependent upon the nature of the system in which the agent is used and the particular type of application technique being employed. Wettable powders containing about 2-5 percent of these surface-active agents are generally prepared. For instance, a typical formulation which has been found to be useful is a wettable powder comprising 65 percent by weight of p-chlorophenoxyacetyl cyanamide, 3t) percent by weight of Barden clay, 2 percent by weight of an oxyalkylated nonylphenol having a molecular weight of about 200 and 3 percent by weight of a lignosulfonate dispersing agent.

Other solid herbicidal compositions containing the cyanamides l as active ingredients are provided in accordance with this invention by dissolving the chemical in a volatile solvent (i.e., acetone) and impregnating this solution upon granular solids such as attapulgite clay, ground vegetable shells, walnut shells and the like. Upon removal of the solvent, potent solid herbicidal formulations are obtained. A typical granular formulation of this type would contain -20 percent by weight ot'the herbicidal ingredient.

Similarly, suspension-type formulations may be conveniently prepared having the substituted eyanamides l as the active ingredients. For instance, an acetone solution of pchlorophenoxyacetyl cyanamide containing one of the abovelisted dispersing agents can be added to water to provide suspensions which are especially suitable for spraying operations.

Emulsifiable concentrates containing the active ingredients I are also readily prepared and are suitable in applying the herbicides to the locus to be protected. These formulations are provided by dissolving the substituted eyanamides in a suitable solvent (e.g., xylene) and adding an appropriate surfactant to the resultant solution which is capable of forming an emulsion kit upon addition to water. Typically, a xylene solution of the ac- I tive ingredient contains about 5 percent by weight of surfac-" tant which advantageously might comprise a mixture of a nonionic surfactant such as oxyalkylated nonylphenol and an anionic surfactant such as an alkylbenzene sulfonate.

Naturally, in order to control the undesirable weed growth, the active ingredient must be applied to the area or locus to be protected in an amount sufficient to exert the desired herbicidal action. Thus, it may be necessary to apply different amounts of the eyanamides l to achieve a desired result depending upon the extent and nature of weed growth, application procedures and other varying features. Generally, it has been found that effective herbicidal action can be obtained by applying the active ingredients of this invention at a rate of about ll0 pounds per acre with an amount of 5 pounds per acre being adequate for most applications. However, high levels of herbicidal activity have been obtained when selected members of the series I have been utilized in even lesser amounts per acre such as one-half to three-fourths pound. The

formulations utilized may contain anywhere from 0.5 percent to about 90 percent by weight of the active ingredient, again depending upon the particular results desired, the methods of application, etc.

What is claimed is:

l. A method for the destruction and inhibition of weeds which comprises applying to the area to be protected, in an amount sufficient to exert a herbicidal action, a compound of the formula wherein R is a chlorinated aryl moiety said aryl group being phenyl, tolyl, xylyl or naphthyl and R" is hydrogen, an alkyl moiety having l-4 carbon atoms, and alkali metal, or a metal of group II in the Periodic Table.

2. The method of claim I wherein said compound is applied to the soil medium as a preemergence herbicide.

3. The method of claim I wherein R" in said compound represents hydrogen.

4. The method of claim 1 wherein R" in said compound represents alkyl having 1-4 carbon atoms.

5. The method of claim 1 wherein R- in said compound represents an alkali metal 6. The method of claim 1 wherein R in said compound represents a metal selected from group II in the Periodic Table.

7. A method for the destruction and inhibition of weeds which comprises applying to the area to be protected in an amount sufficient to exert a herbicidal action a compound of the formula wherein R represents chlorinated phenyl; and R" represents hydrogen, alkyl having l-4 carbon atoms, an alkali metal or a metal of group ll in the Periodic Table.

8. The method of claim 7 wherein said compound is applied to the soil medium as a reemer ence herbicide.

9. The method of c aim 7 w erein R" in said compound represents hydrogen.

10. The method of claim 9 wherein said compound is pchlorophenoxya cetyl cyanamide.

11. The method of claim 7 wherein R" in said compound is alkyl having l-4 carbon atoms.

12. The method of claim 11 wherein said compound is 2,4,5-triehlorophenoxyacetyl-N I 13. The method of claim 7 wherein R" in said compound is -a metal selected from group ll of the Periodic Table.

14. The method of claim 13 wherein said metal in said com pound is zine.

15. A method of selectively destroying weeds in a corn crop which comprises applying to the soil medium surrounding said plants p-chlorophenoxyacetyl cyanamide at a rate sufficient to destroy said weeds substantially without damaging said corn crop.

g gga UNITED STATES PATENT strict CERTIFICATE @F QORREQTWN Patent No. 3 I 535 I 592 Dated T y 18 l 1972 Inventor(s) Herman Breuer It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:

. '1 Title Page, Item No. 73, Assignee "Olin Chemical Co. Inc. is incorrect,

in that it should read -Olin Corporation- (formerly Olin Mathieson Chemical Corporation) The change of name was recorded in the 'U.S. Patent Office on March 9, 1970, on reel 2586, frame 048.

Column 3 Line 42 "hydrides" should read -hydroxides.

Column 4, Line 57, "C H CI N O should read --C H Cl N O Column 6, Line 16, "C H ClN O K" should read --C H ClN O K Column 6, Line 31, "C H CIN O K" should read C H ClN O K.

Column 9, Line 6 of Table I, "dihdrate. should read dihydrate.-.

Column 12, Line 15, "R" is incorrect in that it should read -R"- Column 12 Line 4;], "Z ,4, 5-trichlorophenoxyacetyl-N" is incomplete in that it should read -2 4 5-trichlorophenoxyacetyl- N-methylcyanamide Signed and sealed this 18th day of July 1972 team) it teat? EBWAED IIiFLETCHERJ'R. ROBERT GOTTSCHAIK Attesting Officer" Commissioner of Patents 

2. The method of claim 1 wherein said compound is applied to the soil medium as a preemergence herbicide.
 3. The method of claim 1 wherein R'''' in said compound represents hydrogen.
 4. The method of claim 1 wherein R'''' in said compound represents alkyl having 1-4 carbon atoms.
 5. The method of claim 1 wherein R- in said compound represents an alkali metal
 6. The method of claim 1 wherein R'''' in said compound represents a metal selected from group II in the Periodic Table.
 7. A method for the destruction and inhibition of weeds which comprises applying to the area to be protected in an amount sufficient to exert a herbicidal action a compound of the formula wherein R represents chlorinated phenyl; and R'''' represents hydrogen, alkyl having 1-4 carbon atoms, an alkali metal or a metal of group II in the Periodic Table.
 8. The method of claim 7 wherein said compound is applied to the soil medium as a preemergence herbicide.
 9. The method of claim 7 wherein R'''' in said compound represents hydrogen.
 10. The method of claim 9 wherein said compound is p-chlorophenoxyacetyl cyanamide.
 11. The method of claim 7 wherein R'''' in said compound is alkyl having 1-4 carbon atoms.
 12. The method of claim 11 wherein said compound is 2,4,5-trichlorophenoxyacetyl-N
 13. The method of claim 7 wherein R'''' in said compound is a metal selected from group II of the Periodic Table.
 14. The method of claim 13 wherein said metal in said compound is zinc.
 15. A method of selectively destroying weeds in a corn crop which comprises applying to the soil medium surrounding said plants p-chlorophenoxyacetyl cyanamide at a rate sufficient to destroy said weeds substantially without damaging said corn crop. 